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Charge sensitive optical detection for high throughput study of small molecules

用于小分子高通量研究的电荷敏感光学检测

基本信息

批准号：
8547801
负责人：
NONGJIAN TAO
金额：
$ 21.83万
依托单位：
ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-09-19 至 2015-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8547801
关键词：
Address Antibodies Attention Binding Biochemical Biochemical Reaction Biological Markers Biological Models Biomedical Research Cell division Cell physiology Charge Detection Diagnosis Diagnostics Research Dimensions Disease Drug Industry Drug Targeting Dyes Electrons Enzymes Equipment Event Family Fiber Fluorescence Fluorescent Dyes Genomics Human Ionic Strengths Label Lead Letters Malignant Neoplasms Measurement Measures Membrane Proteins Methods Microscope Molecular Molecular Probes Monitor Mutate Noise Optics Pharmaceutical Preparations Phosphorylation Phosphotransferases Play Positioning Attribute Post-Translational Protein Processing Process Proliferating Proteins Proteomics Reaction Research Role Screening for cancer Signaling Protein Solutions Surface System Techniques Technology Variant Viscosity base cancer cell cancer initiation cancer therapy dalton design drug candidate drug development frontier high throughput screening inorganic phosphate metabolomics new technology optical fiber prevent screening small molecule success theories tool tumor progression

项目摘要

DESCRIPTION (provided by applicant): High-throughput detection of small molecules and post translational protein modifications that involve small molecule biochemical reactions are critical for understanding the mechanisms underlying cancer initiation and progression, for discovering proper biomarkers that enable early cancer detection, and for screening drug candidates for effective cancer treatment. The most widely used technology uses fluorescence labels, which is problematic for small molecules whose sizes are comparable to those of the fluorescent dyes. Various label- free techniques have been developed, but their sensitivity diminishes with the size of the molecules, making it extremely challenging to detect small molecules. To address the need, a charge sensitive optical detection will be developed in this project. The technology is particularly suitable for the detection of small molecules, and biochemical interactions that involve small mass changes. The detection method uses optical probes that compatible with the standard microplate technology, making it attractive for high-throughput detection. The success of the project will lead to a new detection technology to measure small molecule interactions, such as drug-target interactions, membrane protein signaling, protein phosphorylation and other post translational modifications, oxidative and reduction reactions that involves charge transfer. Many of these processes are highly important for the research, diagnostic and treatment of cancer.

描述(申请人提供)：小分子的高通量检测和涉及小分子生化反应的翻译后蛋白质修饰对于了解癌症发生和发展的机制、发现能够早期发现癌症的适当生物标记物以及筛选有效的癌症治疗候选药物至关重要。最广泛使用的技术使用荧光标记，这对尺寸与荧光染料相当的小分子来说是有问题的。各种无标记技术已经被开发出来，但它们的灵敏度随着分子的大小而降低，这使得检测小分子变得极其困难。为了解决这一需求，本项目将开发一种电荷灵敏光学检测装置。该技术特别适用于小分子的检测，以及涉及微小质量变化的生化相互作用。该检测方法使用与标准微板技术兼容的光学探针，使其对高通量检测具有吸引力。该项目的成功将导致一种新的检测技术来测量小分子相互作用，如药物与靶相互作用、膜蛋白信号、蛋白质磷酸化和其他涉及电荷转移的翻译后修饰、氧化和还原反应。其中许多过程对癌症的研究、诊断和治疗非常重要。